{
  "format": "devicerts.manufacturer.v1",
  "cite_as": "Munevo Inc. deviCERTS medical device catalogue. https://devicerts.com/manufacturers/munevo-inc (data as of 2026-11-15).",
  "source": {
    "canonical_url": "https://devicerts.com/manufacturers/munevo-inc",
    "json_url": "https://devicerts.com/manufacturers/munevo-inc.json",
    "markdown_url": "https://devicerts.com/manufacturers/munevo-inc.md",
    "publisher": "deviCERTS (devicerts.com)",
    "data_sources": [
      {
        "registry": "FDA GUDID",
        "url": "https://accessgudid.nlm.nih.gov/"
      },
      {
        "registry": "FDA recalls",
        "url": "https://open.fda.gov/apis/device/recall/"
      }
    ],
    "eudamed_record_synced": null,
    "fda_recalls_as_of": "2026-11-01",
    "registry_facts_computed": "2026-11-15",
    "status_as_of": "2026-11-15",
    "license": "CC BY 4.0",
    "license_url": "https://creativecommons.org/licenses/by/4.0/",
    "license_scope": "The deviCERTS layout and text are licensed under CC BY 4.0. Registry data remain under their source terms: U.S. FDA data (openFDA, AccessGUDID) are U.S. public domain; EUDAMED data are subject to the European Commission reuse terms.",
    "attribution": "DevicErts, https://devicerts.com/manufacturers/munevo-inc",
    "disclaimer": "Compiled by deviCERTS (devicerts.com) from public medical device registries (EUDAMED, European Commission; U.S. FDA via openFDA; AccessGUDID, U.S. National Library of Medicine). deviCERTS is not an official register and gives no regulatory advice: the record in the registry itself prevails."
  },
  "manufacturer": {
    "name": "Munevo Inc.",
    "url": "https://devicerts.com/manufacturers/munevo-inc",
    "registered_as": null,
    "abbreviated_name": null,
    "also_registered_as": [],
    "country": null,
    "country_basis": null,
    "eudamed_status": null,
    "verified": false,
    "roles": [
      "Manufacturer",
      "Part of a group"
    ],
    "registrations": [],
    "identifiers": [
      {
        "label": "DUNS",
        "value": "118704707"
      }
    ],
    "summary": "Munevo Inc. is a medical device manufacturer, with 1 device listed in FDA GUDID (FDA Class I) and 1 FDA recall as of 15 Nov 2026.",
    "noindex": false
  },
  "counts": {
    "devices": 1,
    "devices_note": null,
    "certificates": 0,
    "fda_recalls_matched_by_name": 1,
    "fda_recalls_ongoing": 1,
    "fda_recalls_ongoing_recent": 1,
    "fda_recalls_ongoing_before": null,
    "fda_establishments": 0,
    "sites": 0
  },
  "registry_facts": {
    "covers": "Every device of the manufacturer. A device listed in two registries counts in both.",
    "registries": [
      {
        "registry": "FDA GUDID",
        "devices": 1
      }
    ],
    "device_classes": [
      {
        "class": "FDA Class I",
        "devices": 1
      }
    ],
    "top_emdn_categories": []
  },
  "related": {
    "site_of": null,
    "part_of": {
      "name": "munevo GmbH",
      "url": "https://devicerts.com/manufacturers/munevo-gmbh"
    },
    "sites": [],
    "authorised_representatives": []
  },
  "devices": {
    "shown": 1,
    "total": 1,
    "all_devices_url": "https://devicerts.com/manufacturers/munevo-inc",
    "items": [
      {
        "name": "munevo DRIVE V2",
        "url": "https://devicerts.com/devices/munevo-drive-v2",
        "model_reference": null,
        "device_class": "Class I",
        "registries": [
          "GUDID"
        ],
        "status": "Listed",
        "decision_date": null,
        "open_recall": false
      }
    ]
  },
  "certificates": [],
  "recalls": [
    {
      "number": "Z-2856-2026",
      "classification": "Class II",
      "status": "Ongoing",
      "initiated": "2026-06-19",
      "product_code": "KNN",
      "reason": "A software issue may cause the wheelchair's driving mechanism to fall out of calibration. When this occurs, the device may experience unexpected steering drift or imprecise control while driving the wheelchair. The wheelchair may veer from its intended path, which may cause in low-speed collision, tipping, or injuries to user or bystanders."
    }
  ]
}